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Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.
Soutar AK, Hawkins PN, Vigushin DM, Tennent GA, Booth SE, Hutton T, Nguyen O, Totty NF, Feest TG, Hsuan JJ, et al. Soutar AK, et al. Among authors: feest tg. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7389-93. doi: 10.1073/pnas.89.16.7389. Proc Natl Acad Sci U S A. 1992. PMID: 1502149 Free PMC article.
Renal chloride channel, CLCN5, mutations in Dent's disease.
Cox JP, Yamamoto K, Christie PT, Wooding C, Feest T, Flinter FA, Goodyer PR, Leumann E, Neuhaus T, Reid C, Williams PF, Wrong O, Thakker RV. Cox JP, et al. J Bone Miner Res. 1999 Sep;14(9):1536-42. doi: 10.1359/jbmr.1999.14.9.1536. J Bone Miner Res. 1999. PMID: 10469281 Free article.
Renal tubular acidosis.
Wrong OM, Feest TG. Wrong OM, et al. Among authors: feest tg. N Engl J Med. 1981 Jun 18;304(25):1548-9. doi: 10.1056/NEJM198106183042519. N Engl J Med. 1981. PMID: 7231498 No abstract available.
Erythrocytosis and nephrocalcinosis.
Feest TG, Wrong O. Feest TG, et al. Nephrol Dial Transplant. 1992;7(10):1071. Nephrol Dial Transplant. 1992. PMID: 1331889 No abstract available.
The natural history of distal renal tubular acidosis.
Wrong OM, Feest TG. Wrong OM, et al. Among authors: feest tg. Contrib Nephrol. 1980;21:137-44. doi: 10.1159/000385259. Contrib Nephrol. 1980. PMID: 6771099 No abstract available.
92 results